• Skip to primary navigation
  • Skip to main content
  • Skip to primary sidebar
  • Skip to footer

Cerebral Palsy Scotland

  • Facebook
  • Instagram
  • LinkedIn
  • Home
  • Who we are
    • Our mission and values
    • What we do and why
    • Our story
    • Our team
    • Vacancies
    • Key documents
    • Our centre
  • How we help
    • Therapy for adults
    • Therapy for children
    • Support
    • Training
    • Campaigning
    • Our impact
  • What’s on
    • Events
    • Annual conference
  • Other support
    • Support directories
    • Financial support & equipment funding
    • Advice from parents
    • Online support groups
    • Support for schools
    • Legal support
  • Get information
    • All about cerebral palsy
    • Children
    • Adults
    • Therapy & treatment
    • Oral health
  • News
    • News
    • Blog
  • Get involved
    • Friends of Cerebral Palsy Scotland
    • Raise money
    • Leaving a gift in your Will
    • Corporate partners
    • Philanthropy and major donors
    • Other ways to give
    • Other ways to get involved
    • Shop
    • Trusts
    • Our promise to you

Raising cerebral palsy awareness in education

Debbie Spears from Millburn Academy with a friend

We all know how important it is to raise awareness, whether it is a cause or a disability and there are many ways to make your voice heard.

Let’s turn to cerebral palsy – there are still a lot of people who don’t know what the disability is or how it affects individuals who live with it. Society is getting better at understanding disability but there is more to be done and throughout this blog – I will be talking about how a school marked cerebral palsy awareness day and about how raising awareness in education settings can make a difference.

Earlier this year, Debbie got in touch with us at Cerebral Palsy Scotland to let us know what she had done to mark national cerebral palsy awareness day on 25 March 2022. Debbie lives with cerebral palsy and attends Millburn Academy in Inverness – Debbie was keen on getting her school on board to help raise awareness about her disability – setting out ideas and plans herself for the day.

Debbie and her friend smiling at the camera

Debbie, along with the support of her school, put so much work and thought into the project by making posters with information about the disability and how it affects people including sharing facts. They created a presentation about what cerebral palsy is with a brief explanation using bright colours and images. On the information sheet, there were different links to websites relating to cerebral palsy teenagers including a YouTube clip which fully explains the different aspects of the disability.

All these creations made a difference for the school pupils, helping them to understand what CP is and everyone came together to support the awareness day. The pupils were asked to come into school in non-uniform and to wear green on the day – the colour of cerebral palsy awareness. The presentation was sent out to all the classes and a message went out over the schools tannoy.

We were delighted to hear about this awareness day which was organised by Debbie and as a cerebral palsy charity, a big well done to everyone who put the effort into marking the day – a heartfelt thank you to Debbie and everyone at Millburn Academy.

Cerebral Palsy Scotland welcomes anyone to raise awareness of cerebral palsy. The more people who know of it, the better. We would encourage education settings especially primary and secondary schools to get in touch to find out what they can do like Millburn Academy to raise awareness and educate young people about CP and disability in general. It is very important that pupils understand different things relating to the subject around disability and we can support you to use the right resources.

Get in touch here: getinvolved@cpscot.org.uk

Blog written by Bernie Hunter, Cerebral Palsy Scotland volunteer

 

Craighalbert Centre

Craighalbert Centre  Enabling children in Scotland with neurological conditions (birth-19 years) to reach their potential and fulfil their ambitions through integrated learning, therapy, and care. Providing a range of child- and family-centred programs delivered by highly specialist physiotherapists, occupational therapists, speech therapists, teachers, and learning, care and therapy practitioners.

Policy and campaign update

During the past few months, we have been busy keeping the needs of people with cerebral palsy at the forefront of the minds of statutory service providers and policy makers.

Our CEO, Stephanie Fraser, Chairs the Scottish Government’s National Advisory Committee for Neurological Conditions (NACNC). The committee is focused on ensuring Scottish Government implement the Framework for Action for Neurological Conditions which covers from 2020 – 2025. Cerebral Palsy Scotland has had some funding from this work to look at service provision for adults with CP through our CP Connect programme and this coming year we look forward to working with specific local areas (Health and Social Care Partnerships in Midlothian and in Clackmannanshire and Stirling) to develop this work further in a local setting. Scottish Government published a mid-term progress report on the implementation of the Framework in July: neurological-care-support-framework-action-2020-2025-midpoint-progress-report.pdf (www.gov.scot)

Cerebral Palsy Scotland are also members of the Cross Party Group for Disability in the Scottish Parliament: https://www.parliament.scot/get-involved/cross-party-groups/current-and-previous-cross-party-groups/2021/disability. At their latest meeting, MND Scotland presented the findings of their report on the housing needs for people with MND, some of which is also extremely relevant for people with CP.  You can read their report here: https://aaf1a18515da0e792f78-c27fdabe952dfc357fe25ebf5c8897ee.ssl.cf5.rackcdn.com/2256/MND-Scotland-No-Time-To-Lose-Housing-Report.pdf?v=1646301622000

The All Party Parliamentary Group (APPG) is forum for everyone across the UK to come together at Westminster.  The group’s purpose is to enable policy makers to better understand the challenges faced by individuals of all ages with cerebral palsy and their families. Importantly, it has been constituted to take a life-long approach. The group has already published three reports, the first on early years, the second on best practice in education, health and care, teaching and learning for children with CP schooling and most recently a report on removing barriers for adults. The group is currently calling for evidence with regard to transitioning from children’s to adult services and will meet again in September to discuss this.  To read these reports, you can find them here: https://connectpa.co.uk/appg-cerebral-palsy/

We were delighted to be involved in the Royal Society of Medicine’s conference on 7th July Medicine and Me: Time for a new approach to adults with cerebral palsy with UP – The Adult Cerebral Palsy Movement.  Speakers included contributions from Cerebral Palsy Scotland trustee, Dr Kirsty Colquhoun and CEO, Stephanie Fraser.  A copy of the event recording can be accessed here: https://vimeo.com/732291911/4db25bfc7d

 

As members of the Neurological Alliance of Scotland, Cerebral Palsy Scotland welcomed last month the publication of the first patient survey undertaken by the Neurological Alliances from across the UK.  The report (which can be read here: https://www.scottishneurological.org.uk/news-resources/) highlighted that 1 in 6 people across the UK are living with a neurological conditions and that at least half were continuing to experience delays to accessing appointments and services.  The publication of the survey coincided with Carers’ Week and a debate in the House of Lords on neurological conditions to which our CEO, Stephanie Fraser contributed: https://hansard.parliament.uk/Lords/2022-06-09/debates/B6CB63B1-B491-4A14-B4EF-E6D382CEF6E8/NeurologicalConditions. We look forward to building on this growing evidence to ensure improved data collection so that people with cerebral palsy become more visible to service providers.

Tags: Cerebral Palsy, cerebral palsy scotland

Morag Inglis

Morag is a solicitor with Mitchells Roberton becoming the first female Partner in the firm in 1993. After many years in her role as the Managing Partner, Morag became the first female Chairman of Mitchells Roberton in April 2021. As from 1 April 2025, as a move towards retirement Morag has moved to the role of Consultant: Morag still views people – both clients and colleagues to be at the core of business.

Morag has long been aware of the good work done by Cerebral Palsy Scotland and was delighted to be invited to join the Board as a Trustee in 2022, coinciding with the retirement of her former colleague Donald Reid who was a trustee for many years.

Mitchells Roberton traces its roots back as one of the oldest legal firms in Glasgow and takes pride in the fact that the firm has strong links with and has acted for a number of Glasgow Charitable Organisations.

The chance for Morag to be involved with Cerebral Palsy Scotland fits very well with the fact that Mitchells Roberton has helped families, generation after generation and constantly strives to preserve and strengthen the Mitchells Roberton caring culture within the business.

Morag brings to the Board her broad legal experience: for much of her legal career Morag specialised in areas of commercial practice acting for a wide range of clients in property disposals, acquisitions, leases and in offering a variety of business and general contract advice. Morag also has a large private client base and so gets involved in all sorts of issues for them too. She believes in providing a holistic approach to problem solving always looking at the wider picture.

An interview with Jack Hunter by Jack Hunter

Hello Cerebral Palsy Scotland readers! I hope you are well. My name is Jack Hunter and I’m going interview myself. No, I really am. I’m sitting here writing this at my laptop. I am speaking to you now from the past.

But before I start, I want to thank CP Scotland for their support and this opportunity to promote my new play One of Two, which is premiering at Summerhall, as part of this year’s Edinburgh Festival Fringe.

Ok let’s start:

Hello Jack.

Hello. Good to see you.

What is your connection with CP Scotland?

I am very happy to continue my association with CP Scotland.  And in fact, it goes a long way back. My twin sister Bec and I both have CP, and we used to come all the way down from Inverness to the centre to receive specialist physiotherapy treatment. Of course, that’s when it was known as Bobath Scotland. I still remember going to the centre, when I was wee.  One time In order to measure my gate, the team put dozens of little light bulbs on my body. It kinda looked like a motion capture suit, in a fantasy film. It was so cool! The centre does some fantastic work.

In 2019, I spoke at, what I believe was, the final Bobath Scotland Conference, with the Artistic Director of Birds of Paradise Theatre Company (BOP), Robert Softely Gale – who also has CP. We were speaking about a documentary they had produced in parallel with their 2018 Fringe smash hit My Left Right Foot – The Musical. The film was called You’ve Got to be Ballsy: Stories from the Frontline of Cerebral Palsy and the idea was for me to interview an array of young people with CP, to give them a platform to share their experiences of what being a young disabled person is really like. It was a real privilege to speak with all the people who contributed: artists; swimmers; actors; musicians – and Bec… But you know, I’ve heard all her stuff before… She won’t be happy with that. No, that’s not true. I think for both of us it was a revelatory experience. In fact, if anything it brought us closer.

Through the conversations I had, the aim of the film was to give disabled people, an underepresented group across society, a public platform, to spotlight  discrimination and abelism.. In addition, the filmed participants challenged prevalent  misconceptions about disability. I’m really proud of the film for this reason; as it enabled the  individual voices of young disabled people to be heard. It’s one thing to raise awareness regarding the challenges disabled people face, It’s other to accept the expersonce of every disabled person is diffrent.

Very insightful Jack. Now tell me what is One of Two, what is it about?

One of Two is an autobiographical play that tells my shared story, with Bec, of two twins growing up with Cerebral Palsy. It’s a comedy drama, with shades of light and dark, as well as a lot of lunacy.

On the face of it, we find a very sad Jack (AKA me) alone in his flat, struggling to come to terms with the end of a relationship. He’s trapped in his grotty wee bathroom with a Star Wars inspired “Darth Tater” Mr Potato Head. What’s not funny about that? A revelation occurs to Jack (It’s funny talking about yourself in the third person. You can tell I’ve got the appropriate amount of distance from it now) that he has always needed to be paired with someone else. A friend. A partner. A twin…

Ultimately, the audience will go down the rabbit hole, or perhaps more aptly the toilet pan, with Jack through his shared past with Bec, past on a journey of self-discovery. Creating the show has been a lot of firsts for me. It’s my first ever professional writing credit and it will be my first ever acting job at the fringe – I’ve been living in Edinburgh for nearly ten years, so it’s about time really.

None of this could be possible without the support of a few organisations. Firstly, a big thank you to Summerhall for awarding me the Mary Dick Award. I’m buzzing to be part of their fringe programme. I’m incredibly grateful to Birds of Paradise Theatre Company for their support as producers. I’m excited that Robert Softley Gale is coming on board as director too! I’m sure we’ll have a lot of fun.

I hope that’s enticed you into coming along.

Well… I’ll definitely be there. Why did you want to tell this story?

My relationship with my sister has had an everlasting influence on me and has undoubtedly shaped me as a person. So, in order to understand where I stand in the world, I wanted to unpack this unique relationship.

Without being too cerebral… the play focuses on the disparity of  Bec’s and I’s experience of growing up with CP.  As young kids  our early years were near identical; however as we grew older, key differences have arisen throughout our lives.

You should know that I have a mild manifestation of CP (I walk with a limp as my left leg is shorter than the right), whereas Bec has a slightly more pronounced manifestation (she is a full time wheelchair user).

None of this should matter as people should be able to live their life regardless of their impairment but society has disabled us to varying degrees, Bec more so than me.  I wrote this play because I wanted to investigate this disparity of experience; the inequity of experience between disabled and non-disabled people, but also within the disabled community itself. For instance, Bec and I’s experience within secondary and further education was vastly different. This primarily came down to contrasting attitudes of how educational professionals and fellow students perceived us and our abilities. I think the  play boldly examines the partial failings of our education system and the methods of how it supports young disabled people.

Although the play has a strong theme of disability, it’s also a coming-of-age story, and I hope will have universal appeal with a wide audience, beyond being pigeonholed as a “disabled” story. I know “coming of age” is a bit of a cliché. A bit generic.  A bit bland. But I don’t think it is a style of story often explored from a disabled perspective Bec and I have faced a few barriers throughout our lives; and I think as a society we often are conditioned to not talk about how this impacts our own mental health or self-worth. And at times we are hindered by and urged to adhere to idealistic societal expectations. But in the words of Fleetwood Mac: “you can go your own way…”.

I assume the play will be seen by a predominantly non disabled audience. My hope is that the play will not only raise awareness of the societal barriers that disabled people face, but to provoke the audience into reflecting upon their own perceptions of disability. This is in now way to  alienate the audience. The world, now more than ever, is so polarised. In my mind you’re not going to instigate change by demonsing anyone. I want to bring the audience  with me and keep them on side. How do I do that, you ask? Jokes. Lots of Jokes…..

Wow, how thought provoking!

Why, Thank you.

Why should people come see the show?

First of all, I should say that technically it’s a one man show. On the surface, that doesn’t sound very unique. One person shows are ten a penny at the Fringe. However, Bec will be with me, not in spirit, but through the wonders of multimedia. Voice over, projection and what not. So, she will have a presence. We will converse. And a jolly time will be had by all.

The play has an interesting blend of performative styles. Obviously, it’s theatre. There’s no getting away from that. But that’s not bad in the slightest. It means you can fit in a lot of styles. Not to say that it’s slapdash, you understand. It’s been honed, crafted, and mushed together into a smooth theatrical pulp. The key ingredients are: a slice of silliness, a sprinkle of stand up, and a slurp of spoken word. So hopefully, there’s something for everyone, unless you want interpretive dance. I can’t help you in that department.

However, I do feel that the main selling point of this play is the story. I believe it is truly unique.

What’s your relationship with Bec like?

Oh, we’re incredibly close.  We don’t see each other as much as we used to, what with Bec living in Inverness and me living in Edinburgh. She has a great phrase “It’s a relationship that doesn’t require maintenance” which I think is so true. We can go ages without seeing each other, but the closeness is still the same. I think if you have that shared lived experience, you will always have a tight bond. But we definitely don’t agree on everything.

Having Bec involved in One of Two is incredibly Important to me. Both her and I care immensely about supporting disability rights and raising awareness. Whether it’s through my creative work, or through Bec’s disability training sessions with Naked Brains Consultancy. We want to instigate discussion and social change.

Are there, in your mind, any misconceptions that surround disability?

I think there are probably a fair few floating around. However, I think maybe the biggest dual misconception held by non-disabled people, is that disabled people are either inspiring or destitute. Inspiring because somehow we have defied the odds stacked against us to obtain a ‘normal lifestyle’: job; home; family. That kind of thing. Or we’re destitute, as those that have been disabled by society are left without support and slip through the cracks, leaving them with nothing.

This contrast in views, in my mind, is clearly down to a lack of socio-economic provision to support disabled people, but is also due to a lack of awareness across society. I hope that One of Two can shed some light on this gross inequality.

Thank you, Jack.

You’re welcome.

And finally, when and where can we see One of Two?

One of Two is at Summerhall in Edinburgh, from the 3rd – 28th of August, at 11:45am. The venue has level access, there is audio description and captions at every performance, we are doing four BSL interpreted performances, and one performance will be Relaxed.

If you want any more information, you can follow me on Twitter and Instagram @jack_hunter95, and you can find out full details on the Birds of Paradise website.

Come along, It’s going to be a blast.

Thank you for taking the time to interview with me, Jack.

You’re so welcome.

 

Tags: Cerebral Palsy, cerebral palsy scotland

  • « Go to Previous Page
  • Go to page 1
  • Interim pages omitted …
  • Go to page 17
  • Go to page 18
  • Go to page 19
  • Go to page 20
  • Go to page 21
  • Interim pages omitted …
  • Go to page 55
  • Go to Next Page »

Search

Quick links

  • Ways to give
  • Our mission and values
  • All about cerebral palsy
  • Therapy for adults
  • Therapy for children
  • Campaigning

Copyright © 2025 · Enterprise Pro on Genesis Framework · WordPress · Log in

Cerebral Palsy Scotland logo

Cerebral Palsy Scotland
Bradbury House
10 High Craighall Road
Glasgow, G4 9UD

t: 0141 352 5000
Phone Number for Cerebral Palsy Scotland
Fax Number for Cerebral Palsy Scotland
info@cpscot.org.uk
Email for Cerebral Palsy Scotland
cerebralpalsyscotland.org.uk
Website for Cerebral Palsy Scotland

  • Facebook
  • Instagram
  • LinkedIn
OSCR logo
Nationa Lottery Community Fund logo
Manage Cookie Consent
We use cookies to optimise our website and our service.
Functional cookies Always active
The technical storage or access is strictly necessary for the legitimate purpose of enabling the use of a specific service explicitly requested by the subscriber or user, or for the sole purpose of carrying out the transmission of a communication over an electronic communications network.
Preferences
The technical storage or access is necessary for the legitimate purpose of storing preferences that are not requested by the subscriber or user.
Statistics
The technical storage or access that is used exclusively for statistical purposes. The technical storage or access that is used exclusively for anonymous statistical purposes. Without a subpoena, voluntary compliance on the part of your Internet Service Provider, or additional records from a third party, information stored or retrieved for this purpose alone cannot usually be used to identify you.
Marketing
The technical storage or access is required to create user profiles to send advertising, or to track the user on a website or across several websites for similar marketing purposes.
Manage options Manage services Manage {vendor_count} vendors Read more about these purposes
View preferences
{title} {title} {title}